Temporal Gradients Controlling Embryonic Cell Cycle

Cell proliferation in early embryos by rapid cell cycles and its abrupt pause after a stereotypic number of divisions present an attractive system to study the timing mechanism in general and its coordination with developmental progression. In animals with large eggs, such as <i>Xenopus</i&...

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Main Authors: Boyang Liu, Han Zhao, Keliang Wu, Jörg Großhans
Format: Article
Language:English
Published: MDPI AG 2021-06-01
Series:Biology
Subjects:
Online Access:https://www.mdpi.com/2079-7737/10/6/513
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spelling doaj-9fff213bb85f4a90acb510fa89bb17c02021-06-30T23:44:09ZengMDPI AGBiology2079-77372021-06-011051351310.3390/biology10060513Temporal Gradients Controlling Embryonic Cell CycleBoyang Liu0Han Zhao1Keliang Wu2Jörg Großhans3Center for Reproductive Medicine, Cheeloo College of Medicine, Shandong University, Jinan 250012, ChinaCenter for Reproductive Medicine, Cheeloo College of Medicine, Shandong University, Jinan 250012, ChinaCenter for Reproductive Medicine, Cheeloo College of Medicine, Shandong University, Jinan 250012, ChinaDepartment of Biology, Philipps University, 35043 Marburg, GermanyCell proliferation in early embryos by rapid cell cycles and its abrupt pause after a stereotypic number of divisions present an attractive system to study the timing mechanism in general and its coordination with developmental progression. In animals with large eggs, such as <i>Xenopus</i>, zebrafish, or <i>Drosophila</i>, 11–13 very fast and synchronous cycles are followed by a pause or slowdown of the cell cycle. The stage when the cell cycle is remodeled falls together with changes in cell behavior and activation of the zygotic genome and is often referred to as mid-blastula transition. The number of fast embryonic cell cycles represents a clear and binary readout of timing. Several factors controlling the cell cycle undergo dynamics and gradual changes in activity or concentration and thus may serve as temporal gradients. Recent studies have revealed that the gradual loss of Cdc25 protein, gradual depletion of free deoxyribonucleotide metabolites, or gradual depletion of free histone proteins impinge on Cdk1 activity in a threshold-like manner. In this review, we will highlight with a focus on <i>Drosophila</i> studies our current understanding and recent findings on the generation and readout of these temporal gradients, as well as their position within the regulatory network of the embryonic cell cycle.https://www.mdpi.com/2079-7737/10/6/513embryonic developmentcell cycle remodelingdevelopmental timingmetabolismtemporal gradient
collection DOAJ
language English
format Article
sources DOAJ
author Boyang Liu
Han Zhao
Keliang Wu
Jörg Großhans
spellingShingle Boyang Liu
Han Zhao
Keliang Wu
Jörg Großhans
Temporal Gradients Controlling Embryonic Cell Cycle
Biology
embryonic development
cell cycle remodeling
developmental timing
metabolism
temporal gradient
author_facet Boyang Liu
Han Zhao
Keliang Wu
Jörg Großhans
author_sort Boyang Liu
title Temporal Gradients Controlling Embryonic Cell Cycle
title_short Temporal Gradients Controlling Embryonic Cell Cycle
title_full Temporal Gradients Controlling Embryonic Cell Cycle
title_fullStr Temporal Gradients Controlling Embryonic Cell Cycle
title_full_unstemmed Temporal Gradients Controlling Embryonic Cell Cycle
title_sort temporal gradients controlling embryonic cell cycle
publisher MDPI AG
series Biology
issn 2079-7737
publishDate 2021-06-01
description Cell proliferation in early embryos by rapid cell cycles and its abrupt pause after a stereotypic number of divisions present an attractive system to study the timing mechanism in general and its coordination with developmental progression. In animals with large eggs, such as <i>Xenopus</i>, zebrafish, or <i>Drosophila</i>, 11–13 very fast and synchronous cycles are followed by a pause or slowdown of the cell cycle. The stage when the cell cycle is remodeled falls together with changes in cell behavior and activation of the zygotic genome and is often referred to as mid-blastula transition. The number of fast embryonic cell cycles represents a clear and binary readout of timing. Several factors controlling the cell cycle undergo dynamics and gradual changes in activity or concentration and thus may serve as temporal gradients. Recent studies have revealed that the gradual loss of Cdc25 protein, gradual depletion of free deoxyribonucleotide metabolites, or gradual depletion of free histone proteins impinge on Cdk1 activity in a threshold-like manner. In this review, we will highlight with a focus on <i>Drosophila</i> studies our current understanding and recent findings on the generation and readout of these temporal gradients, as well as their position within the regulatory network of the embryonic cell cycle.
topic embryonic development
cell cycle remodeling
developmental timing
metabolism
temporal gradient
url https://www.mdpi.com/2079-7737/10/6/513
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AT hanzhao temporalgradientscontrollingembryoniccellcycle
AT keliangwu temporalgradientscontrollingembryoniccellcycle
AT jorggroßhans temporalgradientscontrollingembryoniccellcycle
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